Misc Flashcards
Menetrier Disease. Gastric related
Hyperplasia of gastric (stomach) mucosa. Mainly glandular secretion of mucous and super-hypertrophied stomach rugae (look like brain gyri). Parietal cells die, subsequent achlorhydria.
Precancerous
Mallory bodies found on liver biopsy. What are they, and what are their significance?
Eosinophilic inclusions of damaged keratin filaments
Found in alcoholic hepatitis
Aspergillus causes what hepatic abnormality. Mediated by what toxin?
Aflatoxin from aspergillus –> hepatocellular carcinoma
Two places in GI histology with PAS positive intracellar stuff?
Whipple Disease: foamy macrophages with PAS+ inclusions
Alpha-1 antitrypsin deficiency: PAS+ globules in liver
Long-term use of proton-pump inhibitors can cause what metabolic abnormality?
Hypomagnesemia! Ain’t that some shit
Also increased risk for C. diff infection
Orlistat MOA. (Hint: GI related)
Inhibits pancreatic and gastric lipase enzymes resulting in decreased fat absorption. Used in weight-loss treatments. Causes steatorrhea and decreased absorption of fat soluble vitamins
Patient presents with swollen, red, and tender calf. He says he has had a couple of these throughout his body in the last few months. They usually self resolve w/o issue. Also found to have cholestatic LFTs with elevated amylase and lipase. Dx?
Migratory Thrombophlebitis that is strongly associated with pancreatic cancer (hence the cholestatic LFTs with elevated lipase + amylase.
Diseases associated with the infamous HLA-B27 subtype
PAIR: psoriasis, anklyosing spondyolitis, IBD (UC/Crohns), Reiter syndrome (reactive arthritis)
Patient with ADPKD presents with thunderclap headache. After successful treatment, 7 days later develops focal neurologic signs. What happened? What Rx should have been used to prevent this
Subarachnoid hemorrhage from ruptured berry aneurysm (associated with ADPKD). Sequelae of cerebral vasospasm occurring a few days later. Prevent with calcium channel blocker Nimodipine specificaly
Cromolyn sodium use? (Hint: blood cells)
Prevents degranulation of mast cells. Used in asthma prophylaxis (apparently…)
Hemophilia C deficiency and inheritance?
Autosomal recessive deficiency in factor XI.
Contrast with A & B, both X linked
Difference in genetic defect in beta vs alpha thalassemia.
Alpha thalassemia has gene mutations in the gene itself. Beta thalassemia mutations are in promoter and splice site sequences
Basophillic stipiling. What is it? Associated diseases
Aggregates of rRNA that can’t be degraded because of usually lead poisoning (or sideroblastic anemia)
Distinguishing folate deficiency from B12 deficiency using labs
Folate: elevated homocysteine, normal methylmalonic acid
B12: elevated homocysteine & methylmalonic acid
Eculizumab clinical indication
Paroxysmal nocturnal hematuria
Acts to inhibit terminal activation of complement
Ristocetin (old antibiotic, no longer used for Rx humans). Usefulness as a lab test?
Ristocetin causes binding between GpIb and vWF resulting in agglutination
+Ristocetin test in Glanzmann thrombasthenia (defective GpIIb/IIIa)
-Ristocetin test in Bernard-Soulier syndrome (Defective GpIb)
TdT+ marker (flow cytometry). Significance?
Marker of early T and B cells. Think of Acute lymphocytic leukemia (in children)
t(8;14)
c-myc(8) and Ig heavy chain(14)
Burkitt’s lymphoma
t(9;22)
BCR(22) and Abl(9)
Chronic myelogenous leukemia (Rx: Imatinib)
t(11;14)
Cyclin D1(11) and Ig heavy chain(14) Mantle cell lymphoma
t(14;18)
BCL-2(18) and Ig heavy chain(14)
Follicular lymphoma
t(15;17)
M3 subtype of AML that responds to all-trans retinoic acid
Most common type of non-Hodgkin lymphoma in adults?
Diffuse large B-cell lymphoma
JAK2 mutation associated with what blood abnormality
Myeloproliferative disorders: polycythemia vera, essential thrombocytosis, myelofibrosis